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After the treating physician has clinically examined a patient with osteoarthritis of the hip or knee and confirmed that all the inclusion criteria and none of the exclusion criteria are met, the patient will be given the information sheet, a statement of informed consent, and a privacy policy statement for this clinical study.
All Norwegian participants read an information sheet and signed a statement of informed consent approved by the regional ethical committee for medical research (Project ID: S-03116).
Parents were given written and verbal information about the study and a statement of informed consent was signed by the parents of all enrolled children.
The aims of the project and the commitments required were explained by means of an information brochure and all participants signed a statement of informed consent.
The residents of the selected houses were informed of the project objectives and voluntarily signed a statement of informed consent prior to commencing the entomological captures.
Before inclusion, participants were informed of the study procedures and risks, signed a statement of informed consent and were approved for participation by a U.S. EPA physician.
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The participants gave their written statements of informed consent, including the specific consents to use information from HUSK in health research and to link this information with other relevant data sources.
Written statements of informed consent were obtained from all participants at baseline.
All participants signed statements of informed consent as voluntary participants in the study.
The study protocol and statements of informed consent were approved by the Institutional Review Board IRBB) of Drexel University.
The study was approved by the Regional Committee for Medical and Health Research Ethics West, and signed statements of informed consent were obtained from all parents.
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CEO of Professional Science Editing for Scientists @ prosciediting.com